| Tag | Content |
|---|
EnhancerAtlas ID | HS167-03795 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr3:48935330-48936120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr3:48935688-48935699 | AATGTATCAAA | + | 6.02 | | HINFP | MA0131.2 | chr3:48936038-48936050 | CAGCGTCCGCGC | + | 6.22 | | HNF4G | MA0484.1 | chr3:48935336-48935351 | TGGACTTTGGTCCCC | - | 6.39 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGGGATGGA CTTTGGTCCC CAAGCAAAGC ATTAATGAAG GTGTTGCAAG GGGAATAGTT 60
GAGATATGAT ATGAGGAAGA CCAGAGAACA ATTCCTGATG AACGTCCTCC CTCCCAAGCC 120
TCAGTCTGAC CATAGCTTCC TCATCTGGGA GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA 180
GCTGATCACC TTGCTTTCCG TGGAAGGGGC TCGGTCACTG AGGTCATCAT TGCTTCTCAC 240
AGGGATGCCT CTGCCCAGGA GGCTGAGCAG GCCACCGTTG GGTGACAGGC CGAAGAGTGT 300
CAAGTATCTC CCCGGGCCGG GAAAGGTGCG AAAGAGATGG GTACTCTTGC CCCAGGGGAA 360
TGTATCAAAG GACACCTCCA GAACAACCGT ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG 420
CAGGCTTTAC AGGGGACCTG TTTCAACCTT AACGATAATA TTAGTGTTGG CTGAAACCAA 480
AACTATGGAG AGACGTTTAT TCCTTCCCAT CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG 540
ACTGCGGGAC AGGGAACTTT ACATCAGAGC TCTTGACAGG CAGTTAGAGG CTGCTCACTT 600
TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA GGTACAGCTT CCTGCCCACC CCTGAAAGAG 660
AGATTCCCTA GACTTCTCAC GGAAGCTCAC ACATGCCCCT CTTCTGCCCA GCGTCCGCGC 720
CTCGCGGGGG ACCATGCTTT CCGCGCCCCG CCCGGGCCTC CTCCCCAAAG CCTGCGACCC 780
AGCCTCCCGC 790
|
